A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013827



Internal ID21923170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109142946..109143000hg38UCSC Ensembl
chr6:109464149..109464203hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559127
Samples
Known GenesCEP57L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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